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Dual Site-dual Channel Non-invasive Brain Stimulation for Language and Cognitive Function in Stroke Patients

Effect of Dual Site-dual Channel Non-invasive Brain Stimulation for Recovery of Language and Cognitive Function in Stroke Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03486782
Enrollment
30
Registered
2018-04-03
Start date
2018-05-29
Completion date
2020-03-17
Last updated
2020-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke, Aphasia, Cognitive Impairment

Keywords

transcranial direct current stimulation, dual stimulation

Brief summary

The aim of this study is to investigate the effect of dual site-dual channel non-invasive brain stimulation for recovery of language and cognitive function in post stroke patients. Simultaneous dual site-dual channel stimulation was applied by using two sets of transcranial direct current stimulation devices. All subjects will go through four conditions of transcranial direct current stimulation with for 30 minutes. Four conditions are 1) Dual stimulation: i) anodal stimulation on ipsilesional inferior frontal cortex, ii) anodal stimulation on ipsilesional dorsolateral prefrontal cortex. 2) Single stimulation 1: anodal stimulation on ipsilesional inferior frontal cortex and cathodal stimulation on contralesional inferior frontal cortex; 3) Single stimulation 2: anodal stimulation on ipsilesional inferior frontal cortex and cathodal stimulation on contralesional supraorbital area.

Interventions

stimulating inferior frontal cortex with transcranial direct current stimulation for 30 minutes

stimulating dorsolateral prefrontal cortex with transcranial direct current stimulation for 30 minutes

BEHAVIORALaphasia therapy

aphasia therapy for 30 minutes during transcranial direct current stimulation

Sponsors

Samsung Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* left hemisphere involved stroke patients * patients diagnoses as post stroke aphasia

Exclusion criteria

* history of psychiatric disease * patients with metal implants * history of epilepsy * pregnancy * skin defect at the site of electrode attachment

Design outcomes

Primary

MeasureTime frameDescription
Changes in Korean Boston naming testBaseline and after intervention (approximately 2 weeks)measures naming ability thorough picture naming test
Changes in Korean Western Aphasia BatteryBaseline and after intervention (approximately 2 weeks)assessment of language function and provide aphasia quotients

Secondary

MeasureTime frameDescription
Korean Color Word Stroop testBaseline and after intervention (approximately 2 weeks)measures selective attention and executive function
Controlled Oral Word Association TestBaseline and after intervention (approximately 2 weeks)measure verbal fluency
Digit span testBaseline and after intervention (approximately 2 weeks)measures memory span
Changes in brain activation of resting-state and task functional MRIBaseline and after intervention (approximately 2 weeks)Neuroplasticity measure
Changes of Cortical activationBaseline and after intervention (approximately 2 weeks)Cortical activation is measured by functional Near-Infrared-Spectroscopy (fNIRS) (NIRScout, NIRx, Germany)
Korea Montreal Cognitive AssessmentBaseline and after intervention (approximately 2 weeks)measure cognitive function

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026